Epidermal growth factor receptor targeted therapies for solid tumours

Acta Clin Belg. 2011 Jan-Feb;66(1):10-7. doi: 10.2143/ACB.66.1.2062508.

Abstract

The majority of human epithelial cancers is frequently characterized by a functional activation of the epidermal growth factor receptor (EGFR)-driven-pathways. Today, two classes of EGFR inhibitors are routinely used in the clinic: anti-EGFR monoclonal antibodies such as cetuximab and panitumumab and small-molecule inhibitors of the EGFR tyrosine kinase activity such as erlotinib and gefitinib. Anti-EGFR therapies have been approved in several countries for the treatment of metastatic nonsmall-cell lung cancer, colorectal cancer, squamous-cell carcinoma of the head and neck, and pancreatic cancer. This article summarizes the clinical evidence of the anticancer activity of anti-EGFR treatment, and considers the current, and controversial, clinical issues with respect to their optimal use in the treatment of patients with cancer. Mechanisms of resistance to anti-EGFR treatment are also briefly discussed.

Publication types

  • Review

MeSH terms

  • Antibodies, Monoclonal / therapeutic use
  • Antibodies, Monoclonal, Humanized
  • Antineoplastic Agents / therapeutic use
  • Carcinoma, Non-Small-Cell Lung / drug therapy
  • Carcinoma, Squamous Cell / drug therapy
  • Cell Cycle / drug effects
  • Cetuximab
  • Colorectal Neoplasms / drug therapy
  • ErbB Receptors / antagonists & inhibitors
  • ErbB Receptors / drug effects*
  • ErbB Receptors / genetics
  • Glioblastoma / drug therapy
  • Head and Neck Neoplasms / drug therapy
  • Humans
  • Lung Neoplasms / drug therapy
  • Pancreatic Neoplasms / drug therapy
  • Proto-Oncogene Proteins B-raf / genetics
  • Signal Transduction / drug effects

Substances

  • Antibodies, Monoclonal
  • Antibodies, Monoclonal, Humanized
  • Antineoplastic Agents
  • ErbB Receptors
  • BRAF protein, human
  • Proto-Oncogene Proteins B-raf
  • Cetuximab